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Zdrowie i gospodarka · 16/08/2000

FDA Announces Open Meetings for Medical Device Manufacturers to Provide Feedback on Proposed Changes to Registration and Listing Process

The FDA is hosting two public meetings to gather industry input on proposed changes to the medical device registration and listing process and the Medical Device Reporting (MDR) baseline reporting process, with the goal of streamlining data collection and reducing costs.

Source: Federal Register — Food and Drug AdministrationOpen original release →